A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486843



Internal ID264196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97271205..97271520hg38UCSC Ensembl
chr9:100033487..100033802hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027552
Samples
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486843
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer